From Proteopedia
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| + | #REDIRECT [[Tyrosine_kinase]] |
- | [[Image:2xp2.png|left|200px|thumb|Crystal Structure of human anaplastic lymphoma kinase complex with anti-cancer drug, [[2xp2]]]] | + | |
- | {{STRUCTURE_2xp2| PDB=2xp2 | SIZE=350| SCENE= |right|CAPTION= Human anaplastic lymphoma kinase complex with anti-cancer drug, [[2xp2]] }}
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- | '''Anaplastic lymphoma kinase''' (ALK) which is a tyrosine kinase receptor is active in the development of the brain. Chromosomal translocation is observed in ca. 60% anaplastic large-cell lymphomas. The translocation creates a fusion gene composed of the 3’ end of ALK and the 5’ end of nucleophosmin gene. EML4/ALK fusion gene is observed in ca. 4% of non-small-cell lung cancer. Aberrant ALK activity is observed in other carcinomas as well. ALK is comprised by an extracellular domain, a single pass transmembrane domain and an intracellular kinase domain.
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- | == 3D Structures of anaplastic lymphoma kinase ==
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- | Updated on {{REVISIONDAY2}}-{{MONTHNAME|{{REVISIONMONTH}}}}-{{REVISIONYEAR}}
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- | ===ALK kinase domain===
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- | [[2xb7]], [[2xba]], [[3aox]] – hALK + inhibitor – human<br />
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- | [[3l9p]], [[2yhv]], [[2yjr]], [[2yjs]], [[4fnw]], [[4fnx]], [[4anl]] – hALK (mutant)<br />
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- | [[3lcs]] – hALK (mutant) + staurosporine<br />
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- | [[4dce]], [[4fob]], [[4foc]], [[4fod]], [[4fny]], [[4fnz]] – hALK (mutant) + inhibitor<br />
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- | [[3lct]] – hALK (mutant) + ADP<br />
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- | [[2xp2]] – hALK + anti-cancer drug<br />
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- | [[2yfx]], [[4anq]], [[4ans]] – hALK (mutant) + anti-cancer drug<br />
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- | [[Category:Topic Page]]
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Current revision
- REDIRECT Tyrosine_kinase